Redox index of Cys-thiol residues of serum apolipoprotein E and its diagnostic potential

por Yamauchi, Kazuyoshi, Taira, Chiaki, Kawakami, Yasushi
Publicado 2021

A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia

por Taira, Chiaki, Matsuda, Kazuyuki, Arai, Shinpei, Sugano, Mitsutoshi, Uehara, Takeshi, Okumura, Nobuo
Publicado 2017

A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion

por Kaido, Takahiro, Yoda, Masahiro, Kamijo, Tomu, Arai, Shinpei, Taira, Chiaki, Higuchi, Yumiko, Okumura, Nobuo
Publicado 2020

STAT3 gene mutations and their association with pure red cell aplasia in large granular lymphocyte leukemia

por Ishida, Fumihiro, Matsuda, Kazuyuki, Sekiguchi, Nodoka, Makishima, Hideki, Taira, Chiaki, Momose, Kayoko, Nishina, Sayaka, Senoo, Noriko, Sakai, Hitoshi, Ito, Toshiro, Kwong, Yok-Lam
Publicado 2014